Modules | CRAMbridge 4/7

Analytical Method Validation
Sampling Procedure in a GxP Environment
Review of Laboratory Generated Raw Data and Analytical Documents
QC reviewer qualification
Handling and Maintenance of Laboratory Equipment
How to write a good SOP
Pharmacovigilance and Reporting of Adverse Events
Overview of GMP aspects for Senior Management
Introduction to Chemical Reaction Engineering
National Ethical Guidelines for Clinical Trials (ICMR)
Principles on Good Laboratory Practice : OECD 1
General Microbiology Techniques
Basics of Chromatography
Bioanalytical Method Validation
Evaluation of an external service provider/Vendor
Analyst qualification for Quality Control Laboratories
Sample Management in QC Laboratories
Process of Analytical Method Transfer
Practical Guide to Sample Preparation Techniques - Part 1
The Role and Responsibilities of the Study Director in GLP Studies : OECD 8
Arc Flash Safety and Energized Equipment
Hazardous Energies and Lock Out Tag Out Procedures (LOTO)
Liquid Chromatography High Resolution Mass Spectrometry (LCHRMS)
Gas Chromatography Mass Spectrometry (GCMS)